HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1154875Generated: October 28, 2026
Chloroacetyl chloride → HCID 86735835, compound
https://huagongshe.com/reaction/1154875
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | HCID 86735836 | HCID 86735836 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | HCID 86735835 | HCID 86735835 | 79% |
Reaction Steps
To a solution of 2.43 g of ethyl α-ethoxyimino-2-aminothiazol-4-ylacetate hydrobromide in 25 ml of anhydrous N,N-dimethylacetamide is added 1.43 g of chloroacetyl chloride under cooling and stirring. The solution is stirred for 30 minutes under ice-cooling and then for 30 minutes at room temperature. To the reaction mixture is added 150 ml of ethyl acetate and the mixture is repeatedly washed with saturated aq. NaCl solution. The ethyl acetate layer is dried over anhydrous magnesium sulfate, and subjected to the distillation of the solvent under reduced pressure. To the residue is added water to precipitate solid material. The solid is collected by filtration and dried. The procedure gives 1.90 g of ethyl α-ethoxyimino-2-(chloroacetamino)-thiazol-4-ylacetate. Yield 79%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04298606 |
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| Source dataset | uspto-grants-1981_11 |
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| ORD ID | ord-5450f02c866f43aeb5fc427279db6e37 |
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| Source note | uspto-grants-1981_11 |
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